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The validation and usability of remote health home-based fitness assessment test mobile application in adults

The validation and usability of remote health home-based fitness assessment test mobile application in adults

Status
Recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2100045341
Enrollment
Unknown
Registered
2021-04-13
Start date
2021-04-12
Completion date
Unknown
Last updated
2021-11-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Adults

Interventions

APP self home test group:APP self home test
APP Standard test group:APP Standard test
Clinical standard test group:Clinical standard test

Sponsors

Chengdu Shangyi Information Technology Co., LTD
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1.Aged between 18 and 65 years; 2.Own the ability to use smartphone; 3.Obtain the consent of the subject, family member, guardian or legal agent and sign the informed consent.

Exclusion criteria

Exclusion criteria: 1.Rate more than 3 out of 10 on the pain scale; 2.Resting heart rate> 100 bpm; 3.Adjust medicine affecting cardiorespiratory function and heart rate during study period(e.g. Trimetazidine, Bronchodilators, Beta blocker, etc.); 4.Uncontrolled chronic diseses, e.g. hypertension (resting blood pressure >= 160/100mmHg); diabetes (fasting glucose>7.1 mmol/l, HbA1C > 7.0 %); 5.Patients with serious organic disease, such as heart failure with limited activity, unstable angina, a history of myocardial infarction within the past 12 months, or other serious heart disease; 6.Cerebrovascular accident occurred in past 6 months; 7.Patients with active gastrointestinal ulcer, thyroid dysfunction, active tuberculosis; 8.Chronic kidney disease >= 3 stages; 9.Received joints injection or surgery over lower extremities in past 6 months; 10.Poor compliance and have difficulties in cooperating with assessments; 11.Patients who cannot walk independently with assistive device; 12.Patients with psychological disease cannot live independently and cooperate with treatment; 13.A history of alcohol abuse or illegal drug use; 14.Pregnant women, lactating women or pregnant women (including male subjects); 15.Those who had participated in other clinical trials within three months before this trial.

Design outcomes

Primary

MeasureTime frame
Pearson's correlation coefficient;

Secondary

MeasureTime frame
Cardiopulmonary fitness;Muscle strength of upper extremities;Muscle strength of lower extremities;Muscle strength of abdominal muscles;Balance ability;Flexibility;Mobility;Safety;body mass index, BMI;

Countries

China

Contacts

Public ContactLin Yiyi

Chengdu Shangyi Information Technology Co., LTD

linyiyi@postop.cn+86 18683790326

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026